High-Risk Pregnancy

Cleft Lip Repair

I've known about my baby's cleft lip since I was around 30 weeks. I went through the stages of grief but with the Lord's support and my family, I've come to look toward the future and what lies ahead for both of us. I guess being my first daughter after three boys, I wanted her to be perfect. I didn't realize when I first found out that she will be. My question is for mothers who have had babies born with cl/cp. How early did the surgeries start and how many did/has your baby had?

Re: Cleft Lip Repair

  • Hello. My daughter was born with a cleft lip and palate. She is now 10 years old and doing great. She has had several surgeries, however she also had clearing of her palate. She has only had 2-3 for the lip. Depending on which doctor you choose to send her to determends when they will start her surgeries. I believe my daughter was 3 months.
  • Loading the player...
  • ashley0227ashley0227 member
    edited September 2014
    Not clearing.... Clefting... And not "determends".... Auto correct. Sorry.
  • Thank you so much. it's been difficult to find someone who had been through this with their child and the anxiety is killing me! I've been shopping around for a surgeon and craniofacial team but it's overwhelming. thank you for the response.
  • What state are you in? I was alone when I was going through all of it also. When I found out about my daughter, I had to have several ultrasounds. We didn't know the severity until she was born. She always had her entire arm and hand covering her face.
  • I'm a little late to this thread, but I was born with a hemangioma birthmark on my forehead. My surgeon was amazing. I actually didn't start having surgeries until a little later in life, but the earlier the better as it's easier to heal. Where are you located? I highly, highly recommend Boston's Children Hospital.
This discussion has been closed.
Choose Another Board
Search Boards
"
"